rs62143198
This variant is located in the NLRP12 gene.
▶GWAS Catalog Trait Associations (77)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (77)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
DNA-3-methyladenine glycosylase measurement
arf-GAP domain and FG repeat-containing protein 1 measurement
heterogeneous nuclear ribonucleoprotein D-like measurement
RNA-binding protein 3 measurement
clathrin interactor 1 measurement
regulator of microtubule dynamics protein 1 measurement
rho GDP-dissociation inhibitor 2 measurement
beta-adrenergic receptor kinase 1 measurement
5-formyltetrahydrofolate cyclo-ligase measurement
probable RNA-binding protein EIF1AD measurement
About NLRP12
This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Mutations in this gene cause familial cold autoinflammatory syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]
View all NLRP12 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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